State
73,817 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Polaris is recalling about 42,500 model year 2014 Ranger 900 vehicles because a heat shield can fall off, creating fire and burn risks.
GE Appliances is recalling about 222,000 Profile top-loading clothes washers because an electrical component can overheat and cause a fire.
Samsung is recalling Galaxy Note7 smartphones sold before September 15, 2016, because the lithium-ion battery can overheat and catch fire, posing a burn hazard.
Chrysler is recalling specific 2010-2014 models because a module may short circuit, preventing airbags and seat belt pretensioners from deploying in a crash.
Starcraft RV is recalling 40 model year 2017 AR-ONE MAXX LE trailers because the Federal label incorrectly states they have two axles instead of one, creating an overload risk.
Big 5 Sporting Goods is recalling Captiva Designs bungee chairs because rivets can break, posing a fall hazard. Consumers should stop using them and return them for a refund.
Stellar Industries is recalling 3200-series cranes because a valve post may eject and injure nearby people.
FCA US LLC is recalling 2016 Fiat 500 vehicles because the spare tire placard lists an inflation pressure exceeding the tire's maximum limit.
Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because rear seat belt bolts may not be properly tightened.
Amerisource Health Services is recalling 126 cartons of amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain multiple capsules.
Allergy Laboratories is recalling Ephedrine Sulfate Injection vials because an FDA inspection raised concerns about product sterility.
Amerisource Health Services is recalling 115 cartons of 25 mg amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Amerisource Health Services is recalling 2,276 cartons of 10 mg amphetamine tablets because blister cavities may contain more than one tablet.
Aribex Inc is recalling 16,871 NOMAD Pro2 X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, smoke, or ignition.
Aribex Inc is recalling NOMAD Pro X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, melting, smoking, or ignition.
Teva North America is voluntarily recalling 92,480 containers of Linezolid Injection 600 mg/300 mL due to CGMP deviations. The recall covers products distributed nationwide and in Puerto Rico.
Gillig is recalling 2014-2016 Low Floor transit buses because rear brake hoses can fray, potentially causing brake lockup or failure and increasing crash risk.
Bayer Healthcare is recalling 165 Certegra Workstations used with Medrad Stellant CT Injection Systems because they may produce smoke and sparks of fire.
Pharmavite is recalling specific lots of Nature Made adult gummies due to possible Salmonella contamination. Consumers should check lot numbers and stop using the product.
Geneva Foods is recalling Lysander's All Natural Spicy Bourbon Flavor Rub because it contains undeclared soy and wheat allergens and does not declare sulfites.
Hospira Inc. is recalling 357,778 Plum A+ Hyperbaric Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruptions.
Philips Medical Systems is recalling 424 BrightView XCT gamma cameras due to a software defect that may cause the detector to contact patients during specific scans.
Smith & Nephew is recalling Whipknot Soft Tissue Cinch sutures because sterile packaging was breached, compromising sterility. The recall covers 34,065 units distributed worldwide.
Huish Outdoors is recalling Zeagle Grace and Element BCDs because they may leak air, causing loss of flotation and posing a drowning risk to scuba divers.
Riverpoint Medical is recalling sterile nylon surgical sutures because the seals may become open during distribution or packaging.